[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Zonguldak Bulent Ecevit University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":196},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,48,75,102,140,169],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100638992","parasternal-and-adductor-canal-blocks-in-cabg-100638992",false,"NCT07599748","Parasternal and Adductor Canal Blocks in CABG","Comparison of Postoperative Analgesic Efficacy of Parasternal Block and Parasternal Block Combined With Adductor Canal Block in Coronary Artery Bypass Graft Surgery: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients aged 18-80 years Patients classified as American Society of Anesthesiologists (ASA) physical status II-IV Patients scheduled for elective coronary artery bypass graft (CABG) surgery under general anesthesia Patients undergoing saphenous vein graft harvesting during CABG surgery Patients able to understand and use the Numeric Rating Scale (NRS) and Quality of Recovery-15 (QoR-15) questionnaire Patients who provided written informed consent to participate in the study\n\nExclusion Criteria:\n\n* Patient refusal to participate in the study Known allergy or hypersensitivity to local anesthetics, morphine, or study-related medications Emergency coronary artery bypass graft surgery History of chronic opioid use or opioid dependence Pre-existing chronic pain syndromes requiring regular analgesic treatment Cognitive impairment or inability to understand the Numeric Rating Scale (NRS) or Quality of Recovery-15 (QoR-15) questionnaire Coagulopathy or ongoing anticoagulant therapy contraindicating regional anesthesia techniques Local infection at the planned block sites Severe hepatic or renal dysfunction Previous surgery or anatomical abnormality preventing performance of the regional blocks Conversion to a surgical procedure other than planned CABG during the intraoperative period Hemodynamic instability requiring mechanical circulatory support or reoperation in the early postoperative period Patients requiring prolonged postoperative mechanical ventilation or deep sedation preventing postoperative pain assessment","ALL","18 Years","80 Years",{"count":20,"type":21},120,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled trial evaluates the effectiveness of different postoperative analgesic strategies in patients undergoing coronary artery bypass graft (CABG) surgery. Patients were allocated into three groups receiving either conventional analgesia alone, parasternal block in addition to conventional analgesia, or combined parasternal and adductor canal blocks with conventional analgesia. The study aims to compare postoperative pain scores, opioid consumption, and recovery outcomes among the groups in order to determine whether the addition of regional anesthesia techniques, particularly the combined block approach, provides superior analgesia and enhances postoperative recovery following CABG surgery.",[27,28,29],"Postoperative Pain","Regional Anaesthsia","Pain Management",[31,32,33,34],"Coronary artery bypass grafting","Postoperative analgesia","Parasternal block","Adductor canal block","NOT_YET_RECRUITING","2026-05-14",{"date":38,"type":39},"2026-05-20","ACTUAL",{"date":41,"type":21},"2026-06-15",{"date":43,"type":21},"2027-07-31",{"name":45,"class":46},"Zonguldak Bulent Ecevit University","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":47},"100626272","cervical-and-thoracic-mobility-training-in-patients-with-adhesive-capsulitis-100626272","NCT07433478","Cervical and Thoracic Mobility Training in Patients With Adhesive Capsulitis","The Effect of Cervical and Thoracic Mobility Training on Posture, Shoulder Pain, Range of Motion, and Shoulder Functionality in Patients With Adhesive Capsulitis","Inclusion Criteria:\n\n* Diagnosis of unilateral adhesive capsulitis\n* Being between the ages of 20 and 70\n\nExclusion Criteria:\n\n* Presence of glenohumeral joint osteoarthritis, dislocation, subluxation, fracture, tumor\n* Rotator cuff injury\n* Diagnosis of radiculopathy, rheumatological or neurological disease\n* Presence of Thoracic Outlet Syndrome\n* History of surgery on the affected upper extremity\n* Any mental problem that would prevent compliance with tests and exercises","20 Years","70 Years",{"count":58,"type":21},40,[24],"The aim of this study is to investigate the effect of cervical and thoracic mobilization training on posture, shoulder pain, joint range of motion and shoulder function in patients with adhesive capsulitis.",[62],"Frozen Shoulder",[64,65,66],"Frozen shoulder","Adhesizve capsulitis","mobilization","2026-02-25",{"date":69,"type":39},"2026-02-27",{"date":71,"type":21},"2026-04",{"date":73,"type":21},"2026-08",{"name":45,"class":46},{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":22,"phases":85,"briefSummary":86,"conditions":87,"keywords":92,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":100,"leadSponsor":101,"locationsCount":47},"100626003","nerve-gliding-exercises-in-cervical-radiculopathy-100626003","NCT07429981","Nerve Gliding Exercises in Cervical Radiculopathy","Investigation of the Effectiveness of Nerve Gliding Exercises in Individuals With Cervical Radiculopathy","Inclusion Criteria:\n\n* Have been diagnosed with cervical radiculopathy by a specialist physician\n* Have disc herniation at the C5-C6, C6-C7 or C7-T1 level according to imaging (magnetic resonance imaging, MRI) findings (in the bulging or protrusion stage)\n* Have unilateral nerve root involvement\n\nExclusion Criteria:\n\n* Predominance of primary peripheral entrapment neuropathy (carpal\u002Fcubital\u002Fradial tunnel, etc.)\n* Multiple nerve root involvement\n* Progressive neurological deficit\n* History of trauma or surgery to the cervical and upper extremity region\n* Systemic disease contraindicating exercise\n* Pregnancy\n* Manual therapy, injection, or regular physiotherapy applied to the cervical region within the last 3 months\n* Cognitive\u002Fpsychiatric condition preventing compliance with the assessment protocol","55 Years",{"count":84,"type":21},28,[24],"The aim of this study is to investigate the effect of nerve gliding exercises on pain, cervical range of motion, joint position sense, grip strength, functional status and quality of life in individuals with cervical radiculopathy.",[88,89,90,91],"Cervical Radiculopathy at C5 Nerve Root","Cervical Radiculopathy at C6 Nerve Root","Cervical Radiculopathy at C7 Nerve Root","Cervical Radiculopathy",[93,94,95],"Cervical radiculopathy","Neural glide","Neuromobilization","2026-02-18",{"date":98,"type":39},"2026-02-24",{"date":71,"type":21},{"date":73,"type":21},{"name":45,"class":46},{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":109,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":110,"targetDuration":4,"studyType":22,"phases":112,"briefSummary":113,"conditions":114,"keywords":122,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":133,"startDateStruct":135,"completionDateStruct":137,"leadSponsor":139,"locationsCount":4},"100611065","the-effect-of-laughter-yoga-on-individual-and-organizational-outcomes-in-nurse-managers-100611065","NCT07235735","The Effect of Laughter Yoga on Individual and Organizational Outcomes in Nurse Managers","The Effect of Laughter Yoga on Individual and Organizational Outcomes in Nurse Managers: A Longitudinal Study","Inclusion Criteria:\n\n* Currently working as a nurse manager\n* Having at least six months of managerial experience\n* Continuing to serve as a nurse manager throughout the study period\n\nExclusion Criteria:\n\n* Having previously received laughter yoga training\n* Use of medications affecting general health components during the study (e.g., for depression, anxiety)\n* Being pregnant\n* Experiencing an acute stressful life event, such as the death of a close relative\n* Having undergone abdominal surgery within the past 6 months",true,{"count":111,"type":21},80,[24],"The goal of this clinical trial is to learn if laughter yoga can improve both individual and organizational outcomes in nurse managers. The main questions it aims to answer are:\n\n* Does laughter yoga lower burnout and stress levels in nurse managers?\n* Does laughter yoga improve work-life quality and job performance?\n* Does laughter yoga help nurse managers make better decisions and solve problems more effectively?\n* Does laughter yoga lower compassion fatigue and support positive approaches to workplace conflict? Researchers will compare a laughter yoga group with a control group to see if there are meaningful differences.\n\nParticipants will:\n\n* Join structured laughter yoga sessions for a defined period (weekly sessions).\n* Complete surveys before and after the program about stress, burnout, work-life quality, decision-making, problem solving, job performance, compassion fatigue, and conflict approaches.\n* Continue their usual work while attending sessions.",[115,116,117,118,119,120,121],"Burnout, Professional","Stress, Psychological","Compassion Fatigue","Quality of Life","Decision Making","Problem Solving","Work Performance",[123,124,125,126,127,119,120,128,117,129,130,131],"Nurse Managers","Laughter Yoga","Burnout","Stress","Work-Life Balance","Job Performance","Conflict Management","Organizational Outcomes","Professional Development","2025-11-17",{"date":134,"type":39},"2025-11-19",{"date":136,"type":21},"2025-12-11",{"date":138,"type":21},"2026-03-17",{"name":45,"class":46},{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":145,"acronym":4,"eligibilityCriteria":146,"healthyVolunteers":11,"sex":147,"minAge":17,"maxAge":148,"enrollmentInfo":149,"targetDuration":4,"studyType":22,"phases":151,"briefSummary":152,"conditions":153,"keywords":157,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":132,"lastUpdatePostDateStruct":162,"startDateStruct":164,"completionDateStruct":166,"leadSponsor":168,"locationsCount":47},"100611910","ipp-psp-block-vs-spsipb-in-breast-surgery-100611910","NCT07246720","IPP-PSP Block vs. SPSIPB in Breast Surgery","Interpectoral-pectoserratus Plane Block vs. Serratus Posterior Superior Intercostal Plane Block for Postoperative Analgesia in Patients Undergoing Breast Cancer Surgery","Inclusion Criteria:\n\n* 18-65 years of age\n* ASA I-II-III risk groups\n* Patients with informed consent\n* Patients undergoing breast cancer surgery\n\nExclusion Criteria: • Ages \\\u003C18 and \\>65\n\n* ASA ≥ IV\n* History of allergy to local anesthetics\n* Known coagulation disorders\n* Infection near the insertion site\n* Chronic analgesic use\n* Patients with diabetes mellitus and those receiving neoadjuvant chemotherapy (due to potential impairment of pain sensation)\n* Body mass index \\>30\n* Dementia or confusion\n* Lack of cooperation","FEMALE","65 Years",{"count":150,"type":21},70,[24],"This prospective, randomized clinical study aims to compare the analgesic efficacy of the interpectoral-pectoserratus plane block and the serratus posterior superior intercostal plane block for postoperative pain management in patients undergoing breast cancer surgery. Both techniques are ultrasound-guided regional anesthesia methods targeting different interfascial planes of the thoracic wall. The study will evaluate postoperative pain scores, opioid consumption, Quality of recovery and potential complications. The findings are expected to contribute to optimizing regional anesthesia strategies for enhanced recovery and improved analgesia following breast cancer surgery.",[154,155,156],"Postoperative Acute Pain","Breast Cancer","Regional Anesthesia",[158,159,160,161,29],"Interpectoral-Pectoserratus Plane Block","Serratus Posterior Superior Intercostal Plane Block","Breast Cancer Surgery","Opioid Consumption",{"date":163,"type":39},"2025-11-24",{"date":165,"type":21},"2025-11-15",{"date":167,"type":21},"2026-06-30",{"name":45,"class":46},{"id":170,"slug":171,"hasResults":11,"nctId":172,"briefTitle":173,"officialTitle":173,"acronym":4,"eligibilityCriteria":174,"healthyVolunteers":109,"sex":16,"minAge":175,"maxAge":176,"enrollmentInfo":177,"targetDuration":4,"studyType":22,"phases":179,"briefSummary":180,"conditions":181,"keywords":183,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":188,"lastUpdatePostDateStruct":189,"startDateStruct":191,"completionDateStruct":193,"leadSponsor":195,"locationsCount":4},"100573260","0-3-months-infantile-colic-the-effect-of-ocean-sound-on-babies-100573260","NCT06743971","0-3 Months Infantile Colic The Effect of Ocean Sound on Babies","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* Diagnosis of infantile colic according to Wessel criteria\n* The baby is born prematurely\u002Fmaturely\n* The baby is between 0-3 months\n* Babies must have passed the newborn hearing screening test (the sound level used during the test is set at 30 decibels)\n* Otoscopic examinations of babies should be performed by a specialist physician\n* The baby has no diagnosis other than infantile colic on examination\n* The baby does not have any chronic disease\n* Mothers know how to read, write and speak Turkish\n* No alternative application (massage, oil, herbal teas, etc.) should be used before the application\n\nExclusion Criteria:\n\n* The baby has any acute and chronic disease\n* The baby has a congenital anomaly\n* The mother has diagnosed mental and psychological problems\n* Diagnosis of lactose intolerance in infants by a physician\n* Previously diagnosed with Infantile Colic and continuing medical treatment\n* Babies have not passed the newborn hearing screening test\n* Otoscopic examinations of infants not performed by a specialist physician","0 Days","3 Months",{"count":178,"type":21},60,[24],"Infant colic is one of the most common health problems in newborns and infants. It is a syndrome of unknown cause, occurring in attacks, weakened by clenched fists, hardening of the abdomen, flatulence, pulling the legs to the abdomen, very difficult to stop and excessive crying. Various studies have been conducted on this subject and the incidence rates in healthy babies vary between 10-40%. Significant behavioral problems may arise in sleep, rest and feeding due to frequent and prolonged periods of arrest, which are considered to be the upper point of normal crying. In these mothers, symptoms such as helplessness, fatigue, insomnia, exhaustion, loss of life, feelings of inadequacy, anxiety and crying problems may occur. In these mothers, variability is also extended. While in the womb, the fetus is attuned to the sound of the blood in the mother's arteries and the rocking motion of her abdomen. During infancy, the uterus is constantly hearing sounds at a higher frequency than a vacuum cleaner and these sounds stimulate a calming reflex in the baby. Our aim in this study was to investigate the sound of the ocean in infants with infantile colic aged 0-3 months.",[182],"Infantile Colic",[184,185,186,187],"pediatric nurse","infantil colic","cry","sleep","2024-12-16",{"date":190,"type":39},"2024-12-20",{"date":192,"type":21},"2024-12-15",{"date":194,"type":21},"2025-01-30",{"name":45,"class":46},""]